Home / 510(k) Clearances / K972032

510(k) K972032

VISUALINE II METHAMPHETIMINE by Sun Biomedical Laboratories, Inc. — Product Code DKZ

K972032 is an FDA 510(k) premarket notification submitted by Sun Biomedical Laboratories, Inc. for the device "VISUALINE II METHAMPHETIMINE". The FDA issued a decision of Substantially Equivalent on August 12, 1997. The device falls under product code DKZ (Enzyme Immunoassay, Amphetamine), a Class II device regulated under 21 CFR 862.3100. Sun Biomedical Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 12, 1997
Date Received
June 2, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Amphetamine
Device Class
Class II
Regulation Number
862.3100
Review Panel
TX
Submission Type

Other clearances by Sun Biomedical Laboratories, Inc.

  • K023856 — VISUALINE METHADONE DIPSTRIPTEST (August 25, 2003)
  • K023648 — VISUALINE CUP IV FOR DRUGS OF ABUSE TEST FOR QUALITATIVE DETERMINATION OF COCAIN (May 6, 2003)
  • K014089 — VISUALINE II (ALSO KNOWN AS SUNLINE) BARITURATES (April 25, 2002)
  • K020136 — VISUALINE BARBITURATES DIPSTRIP TEST (March 20, 2002)
  • K011499 — VISUALINE AMPHETAMINE DIPSTRIP ASSAY (July 17, 2001)
  • K010177 — VISUALINE II (ALSO KNOWN AS SUNLINE) AMPHETAMINE ASSAY (May 17, 2001)
  • K993485 — VISUALINE V DRUGS OF ABUSE DIPSTRIP PANEL FOR QUALITATIVE DETERMINATION OF COCAI (December 27, 1999)
  • K983790 — VISUALINE II (ALSO KNOWN AS SUNLINE) PHENCYCLIDINE (March 1, 1999)
  • K981314 — VISUALINE II (ALSO KNOWN AS SUNLINE) METHADONE (September 4, 1998)
  • K963606 — VISUALINE COMBO V (COCAINE/THC) TEST (October 30, 1996)

Other clearances for product code DKZ

  • K240670 — DRI Ecstasy Plus Assay (October 30, 2024)
  • K233019 — AllTest Multi-Drug Rapid Test Cup; AllTest Multi-Drug Rapid Test Panel; AllTest (December 13, 2023)
  • K231137 — Xenta Drug Screen Cup, Xenta Drug Screen Dipcard (May 19, 2023)
  • K200363 — Quidel Triage® TOX Drug Screen, 94600 (March 11, 2020)
  • K191099 — Atlas Multi-Drugs Screening Test Cup, Atlas Multi-Drugs Screening Test Panel (October 3, 2019)
  • K182719 — Quidel Triage TOX Drug Screen, 94600; Quidel Triage® MeterPro (June 19, 2019)
  • K182738 — Single and Multi-Drug Rapid Test Panel With Adulteration (Urine), Single and Mul (March 27, 2019)
  • K180879 — BIO-VENTURE Rapid Multi-Drug Test Easy Cup for OTC Use, BIO-VENTURE Rapid Multi- (December 14, 2018)
  • K181945 — QuickScreen Pro Multi Drug Screening Test, Model 9395Z (October 18, 2018)
  • K173303 — INSTANT-VIEW plus Multi-Drug of Abuse Urine Test - Simple Cup (OTC Use), INSTANT (February 23, 2018)

FDA data resources